Meet Rimma, this little girl can no longer smile, cannot say simple words, cannot hold and turn her head. A terrible and extremely rare genetic disease is killing this fragile flower day by day, taking away her memories, her ability to move and communicate. Very soon Rimmusya may stop seeing and even breathing.

Conventional medicines will not help, because the disease was caused by a gene failure. So the only way to save the child is to develop a special gene replacement treatment. Such treatment could stop the development of the disease and save the child's life. The medicine will soon be available on the market, but will Rimma be able to get it? Or will she remain a prisoner in her own immobile body forever?

At present, the girl's parents cannot pay the full cost of treatment, as it costs up to 2,000,000 euros. With titanic efforts, the family managed to find a quarter of the amount, but their financial resources are exhausted - they cannot cope further without help and support.

Rimma has only a few years to stop the disease, otherwise the damage to her brain and nervous system may be so severe that the girl cannot be saved. It is very important that Rimma does not lose precious time and receives treatment as soon as it becomes available on the medical market.

Dear friends, let's help Rimma become one of the first patients in the world to overcome such a rare and dangerous disease. Don't be intimidated by the amount of money needed for treatment - together we can save the girl. All it takes is a small donation and sincere faith in Rimma's victory! Please support the girl!

07.07.2025

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